Canonical Allele Identifier: CA469805619

Gene: MYPN

Linked Data

• dbSNP Id: rs1224300334
• gnomAD v4: 10-68166298-T-C
• MyVariant Identifiers: chr10:g.69926055T>C (hg19) ; chr10:g.68166298T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166298T>C , CM000672.2:g.68166298T>C	GRCh38
NC_000010.10:g.69926055T>C , CM000672.1:g.69926055T>C	GRCh37
NC_000010.9:g.69596061T>C	NCBI36
NG_032118.1:g.65182T>C , LRG_410:g.65182T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.780T>C	ENSP00000346369.2:p.Asn260=
ENST00000373675.4:c.1605T>C	ENSP00000362779.4:p.Asn535=
ENST00000540630.6:c.1659T>C	ENSP00000441668.3:p.Asn553=
ENST00000613327.5:c.1605T>C	ENSP00000480757.2:p.Asn535=
ENST00000687572.1:c.483T>C	ENSP00000510427.1:p.Asn161=
ENST00000687705.1:c.*1854T>C	ENSP00000509639.1:n.*1854T>C
ENST00000688812.1:c.1581T>C	ENSP00000510658.1:p.Asn527=
ENST00000689002.1:n.657T>C
ENST00000690544.1:c.*876T>C	ENSP00000508989.1:n.*876T>C
ENST00000358913.10:c.1605T>C MANE Select	ENSP00000351790.5:p.Asn535=
ENST00000354393.6:c.780T>C	ENSP00000346369.2:p.Asn260=
ENST00000358913.9:c.1605T>C	ENSP00000351790.5:p.Asn535=
ENST00000540630.5:c.1605T>C	ENSP00000441668.2:p.Asn535=
ENST00000613327.4:c.723T>C	ENSP00000480757.1:p.Asn241=
NM_001256267.1:c.1605T>C	NP_001243196.1:p.Asn535=
NM_001256268.1:c.723T>C	NP_001243197.1:p.Asn241=
NM_032578.3:c.1605T>C , LRG_410t1:c.1605T>C	NP_115967.2:p.Asn535=
NR_045662.3:n.1032T>C
NR_045663.3:n.1873T>C
XM_006718043.2:c.1659T>C	XP_006718106.1:p.Asn553=
XM_011540292.1:c.1635T>C	XP_011538594.1:p.Asn545=
XM_017016833.1:c.1683T>C	XP_016872322.1:p.Asn561=
XM_017016834.2:c.1605T>C	XP_016872323.1:p.Asn535=
XM_024448236.1:c.483T>C	XP_024304004.1:p.Asn161=
NR_045662.4:n.1142T>C
NR_045663.4:n.1818T>C
NM_001256267.2:c.1605T>C	NP_001243196.1:p.Asn535=
NM_001256268.2:c.723T>C	NP_001243197.1:p.Asn241=
NM_032578.4:c.1605T>C MANE Select	NP_115967.2:p.Asn535=